850026-81-2

Upstream product

• 132969-60-9 (2S)-3-[(4-methoxybenzyl)oxy]-2-methylpropanal 
• 101712-01-0 (S)-1-((S)-4-benzyl-2-oxo-oxazolidin-3-yl)-2-methylpentane-1,3-dione 
• 850026-69-6 (2S,4R,5S,6S)-1-[(S)-4-benzyl-2-oxooxazolidin-3-yl]-5-hydroxy-7-(4-methoxybenzyloxy)-2,4,6-trimethylheptane-1,3-dione 
• 850026-77-6 (R)-2-[(4S,5S,6S)-6-[(S)-2-(4-methoxybenzyloxy)-1-methylethyl]-2,2,5-trimethyl-1,3-dioxan-4-yl]-1-propanol 

Downstream Products

• 140925-55-9 (3R,4S,5S,6S)-7-Benzyloxy-2,4,6-trimethyl-hept-1-ene-3,5-diol 
• 140925-78-6 C₂₀H₃₀O₃ 
• 1419186-75-6 C₂₀H₃₂O₄ 
• 1419186-84-7 C₂₀H₃₂O₄ 
• 1419186-85-8 C₂₀H₃₀O₄ 
• 1419186-71-2 C₂₁H₃₂O₃ 
• 1419186-73-4 C₂₅H₄₁NO₇ 
• 1419186-74-5 C₂₆H₄₃NO₇ 
• 116661-41-7 (2S,4R,5R)-1-(benzyloxy)-5-hydroxy-2,4,6-trimethylhept-6-en-3-one 
• 1419186-72-3 C₂₉H₄₅NO₆S₂ 
• 1189568-53-3 C₄₃H₇₄O₉Si 
• 1189568-54-4 C₄₃H₇₄O₉Si 
• 850026-89-0 (3S,4R,5S,6S)-2-[(3S,4R)-3-ethyl-4-hydroxy-1-pentynyl]-2-methoxy-6-[(S)-2-(4-methoxybenzyloxy)-1-methylethyl]-3,5-dimethyltetrahydropyran-4-ol 
• 850026-97-0 (2S,3R,4R,5S,6R,8R,9S)-9-ethyl-2-[(S)-2-(4-methoxybenzyloxy)-1-methylethyl]-3,5,8-trimethyl-1,7-dioxaspiro[5.5]undec-10-en-4-yl acetate 

Relevant academic research and scientific papers

Formal total synthesis of spirangien A

A formal total synthesis of the spiroketal containing cytotoxic myxobacteria metabolite spirangien A (1) is described. The approach utilizes a late introduction of the C20 alcohol that mirrors the biosynthesis of this compound. The key steps involved a hi

Total synthesis of ( - )-spirangien A, an antimitotic polyketide isolated from the myxobacterium Sorangium Cellulosum

An expedient first total synthesis of (-)-spirangien A, a potent cytotoxic and antifungal polyketide of myxobacterial origin, is described. By using a common 1,3-diol intermediate obtained by an efficient aldol-reduction sequence for installation of the C

Total synthesis of pteridic acids A and B

Pteridic acid A (1) is a spirocyclic octaketide produced by the phytoepiphytic actinomycete Streptomyces hygroscopicus TP-A0451 and possesses potent plant-growth-promoting activity comparable to that of indole-3-acetic acid. The enantioselective total syn

Enantioselective total synthesis of pteridic acid A

Pteridic acid A, a potent plant growth promoter with auxin-like activity, was synthesized enantioselectively by using the Evans asymmetric aldol reaction as the key C-C bond forming step. The Royal Society of Chemistry 2005.